Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,904 recalls have been distributed to Ohio in the last 12 months.
Showing 28401–28420 of 30,087 recalls
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is labeled in part "***Surgical Laser Technologies Recalled by...
The Issue: Firm became aware that some products within the specified lot may not have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is Recalled...
The Issue: Animas has identified a component issue affecting a small supply of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine...
The Issue: Thru hole at the tip of the screw is undersized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for...
The Issue: Lumenis Ltd is recalling certain models of VersaCut Morcellator devices to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Hybrids Recalled by Diagnostic Hybrids Inc Due to RhMK product...
The Issue: RhMK product fungal contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is including additional information and instructions in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage:...
The Issue: Veridex, LLC has received a report that a patient's demographics were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage:...
The Issue: Veridex, LLC has received a report that a patient's demographics were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABC(R) NOZZLE Recalled by ConMed Corporation Due to ConMed received...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...
The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade Recalled by ConMed...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROSURGICAL ENT NEEDLE ELECTRODE Recalled by ConMed Corporation Due to...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraClean(R) Accessory Electrode 4 inch Coated Blade with Extended...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.